Process Engineer Viral Vectors | Prozess Ingenieur Virale Vektoren (m/w/d), Herbert-Bayer-Straße 8
ProBioGen AG
Job Summary
This role involves supporting the development and GMP production of sterile, viral drug products for clinical studies. The Process Engineer will be responsible for the execution and monitoring of aseptic filling processes and visual inspections, ensuring strict adherence to EU GMP Annex 1. Key day-to-day tasks include manufacturing sterile viral pharmaceuticals using state-of-the-art equipment, coordinating vial integrity testing, and maintaining comprehensive GMP-compliant documentation such as SOPs and material specifications. A critical component of the job is continuous quality and process optimization to improve throughput and process times. The position requires a degree in a natural science field (Biotechnology, Bioprocess Engineering, Biochemistry) and a willingness to work with genetic safety level 2 organisms (viruses). This is an attractive opportunity within a growing BioTech company focused on innovative therapeutic developments, offering a collaborative culture and continuous professional development.
Required Skills
Education
Completed university degree in Natural Sciences (Biotechnology, Bioprocess Engineering, Biochemistry) or comparable qualification
Experience
- Professional experience in a GMP production environment (advantageous)
- Experience in sterile filling (advantageous)
- Experience with Aseptic Process Simulation/Mediafill (advantageous)
- Experience working in a Cleanroom B environment
- Experience working with viruses or viral vectors (desirable)
Languages
Additional
- Willingness to work with organisms of genetic safety level 2 (viruses)
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